Monocytes from Cystic Fibrosis Patients Are Locked in an LPS Tolerance State: Down-Regulation of TREM-1 as Putative Underlying Mechanism

Cystic Fibrosis (CF) is an inherited pleiotropic disease that results from abnormalities in the gene that codes for the chloride channel, Cystic Fibrosis Transmembrane Conductance Regulator (CFTR). CF patients are frequently colonized by several pathogens, but the mechanisms that allow colonization...

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Главные авторы: del Fresno, Carlos, Gómez-Piña, Vanesa, Lores, Vanesa, Soares-Schanoski, Alessandra, Fernández-Ruiz, Irene, Rojo, Blas, Alvarez-Sala, Rodolfo, Caballero-Garrido, Ernesto, García, Felipe, Veliz, Tania, Arnalich, Francisco, Fuentes-Prior, Pablo, García-Río, Francisco, López-Collazo, Eduardo
Формат: Artigo
Язык:Inglês
Опубликовано: Public Library of Science 2008
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Research Article
Online-ссылка:https://ncbi.nlm.nih.gov/pmc/articles/PMC2442190/
https://ncbi.nlm.nih.gov/pubmed/18628981
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0002667
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